International Regulatory Affairs Specialist - San Jose

The Regulatory Affairs Specialist is a key partner to R&D, Quality, Manufacturing, and Marketing teams, responsible for driving regulatory strategy and ensuring compliance with global medical device regulations. · ...

The Regulatory Affairs Specialist drives regulatory strategy and ensures compliance with global medical device regulations. · ...

The Regulatory Affairs Specialist is a key partner to R&D, Quality, Manufacturing, and Marketing teams, · responsible for driving regulatory strategy and ensuring compliance with global medical device regulations. · Develop regulatory strategies for new product introductions and ...

+ Job Overview · Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. · +Bachelor's Degree in Lifescience or related discipline. · At least ...

Regulatory Affairs Specialist at IQVIA prepares regulatory submissions documents to support clinical trial and marketing authorization activities. · ...

Under general supervision Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients Provides regulatory support for assigned projects. · ...

The Regulatory Affairs Specialist prepares and documents regulatory submissions to government agencies. They work on problems of diverse scope where analysis of situations or data requires a review of identifiable factors. · ...

The Regulatory Affairs Specialist supports global regulatory strategy and execution for medical device products ensuring compliance with FDA and international regulations throughout the product lifecycle. · ...

The Regulatory Affairs Specialist supports global regulatory strategy and execution for medical device products ensuring compliance with FDA and international regulations throughout the product lifecycle. · This role partners closely with R&D Quality Manufacturing and Clinical te ...

We are hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara location.This new team member will combine knowledge of scientific regulatory business issues to enable products including combination products that are developed manufactured or distributed to m ...

We are presently hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara CA location. Prepares robust regulatory applications to achieve departmental and organizational objectives. ...

+ Work that matters · Grow and learn · Care for yourself and your family · Be your true self+Career development with an international company where you can grow the career you dream of. · Excellent retirement savings plan with high employer contribution. · Tuition reimbursement · ...

This role provides compliance support to the Regulatory Affairs organization by driving preparation of KPI dashboards,promoting quality system integration for acquisitions,new product introductions. · Driving preparation of KPI dashboards,maintaining formal RA management review m ...

We are currently seeking a Staff Regulatory Affairs Specialist, Pharmaceuticals to join our Endoscopy Division to be based in San Jose, CA or remotely anywhere within the United States. · What You Will Do · As Staff Regulatory Affairs Specialist, Pharmaceuticals, on the Pre-Marke ...

Work Flexibility: RemoteWe are currently seeking a Staff Regulatory Affairs Specialist, Pharmaceuticals to join our Endoscopy Division to be based in San Jose, CA or remotely anywhere within the United States. · What you will do · As Staff Regulatory Affairs Specialist, Pharmaceu ...

Title: Senior Regulatory Affairs Specialist · Location: Santa Clara, CA · Duration: 9+ Months · Responsibilities · Must have 3-5 years of experiences in Medical Device Regulatory Affairs · Needs to have experience in Regulatory Change Assessment for Class III medical devices and ...

· Company Description · Pharmaceutical / Biotech · Job Description · SR. REGULATORY AFFAIRS SPECIALIST  · Santa Clara, CA  · Pharmaceutical / Biotech · EXP 7-10 yrs · DEG Bach · Relo · Bonus · Job Description · We are searching for an experienced regulatory professional to work ...

Title: Senior Regulatory Affairs Specialist · Location: Santa Clara, CA · Duration: 9+ Months · Responsibilities: · Must have 3-5 years of experiences in Medical Device Regulatory Affairs · Needs to have experience in Regulatory Change Assessment for Class III medical devices and ...

We are hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara, CA location.As an individual contributor, this new team member will combine knowledge of scientific, regulatory and business issues to enable products... · ...

· Company Description · Pharmaceutical / Biotech · Job Description · SR. REGULATORY AFFAIRS SPECIALIST  · California Santa Clara · EXP 7-10 yrs · DEG Bach · RELO · BONUS · Job Description. · We are searching for an experienced regulatory professional to work within the Companion ...